2010
DOI: 10.1016/j.ajhg.2010.08.002
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Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism

Abstract: Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC) is a neurodegenerative disease marked by early-onset cataract and hearing loss, retinitis pigmentosa, and involvement of both the central and peripheral nervous systems, including demyelinating sensorimotor polyneuropathy and cerebellar ataxia. Previously, we mapped this Refsum-like disorder to a 16 Mb region on chromosome 20. Here we report that mutations in the ABHD12 gene cause PHARC disease and we describe the clinical manifes… Show more

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Cited by 187 publications
(208 citation statements)
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References 24 publications
(35 reference statements)
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“…46 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC), a syndrome similar to Refsum disease, is caused by mutations in ABHD12. 47 Coenzyme Q10 (CoQ10) deficiency is often associated with seizures, cognitive decline, pyramidal track signs, and myopathy but may also include prominent cerebellar ataxia. 48,49 The symptoms may respond to CoQ10 treatment.…”
Section: Reviewmentioning
confidence: 99%
“…46 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC), a syndrome similar to Refsum disease, is caused by mutations in ABHD12. 47 Coenzyme Q10 (CoQ10) deficiency is often associated with seizures, cognitive decline, pyramidal track signs, and myopathy but may also include prominent cerebellar ataxia. 48,49 The symptoms may respond to CoQ10 treatment.…”
Section: Reviewmentioning
confidence: 99%
“…In this regard, FAAH polymorphisms have been associated with drug abuse behaviours [90,91]. A recent proof of concept of this notion is the involvement of ABDH12 mutations that associate with the neurodegenerative disease polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataract (PHARC) that occurs with concomitant demyelination and cerebellar ataxia [92]. CB 1 receptor signalling can be influenced as well by prenatal exposure to marijuana-derived cannabinoids or by contact with drugs targeting either directly or indirectly the ECB system.…”
Section: Pathophysiological Implications Of the Neurodevelopmental Romentioning
confidence: 99%
“…The effects of spinal or supra-spinal administration of JZL184 on nociceptive processing in control rats, or in models of chronic pain have yet to be reported. In the context of chronic pain states involving the activation of spinal glial cells, it is noteworthy that 2-AG signalling in microglia is thought to be terminated by ABHD12 [96], which is not sensitive to JZL184 [97].…”
Section: -Ag and Pain Processingmentioning
confidence: 99%